|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any functional anomaly of a primary cilium which contains a variable array of axonemal microtubules but does not contain molecular motors; nonmotile primary cilia are found on many different cell types and function as sensory organelles that concentrate and organize sensory signaling molecules (Mammalian Phenotype Ontology, MP_0013211)|
|Downloads & Tools|
1 gene mutations causing the abnormal nonmotile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|PKD1||polycystic kidney disease 1 (autosomal dominant)|